Canonical Allele Identifier: CA552864109

Gene: SPP1

Linked Data

• dbSNP Id: rs1270211749
• gnomAD v2: 4-88903097-CAA-C
• gnomAD v3: 4-87981945-CAA-C
• gnomAD v4: 4-87981945-CAA-C
• MyVariant Identifiers: chr4:g.88903098_88903099del (hg19) ; chr4:g.87981946_87981947del (hg38)

Genomic Alleles

HGVS	Genome Assembly
NC_000004.12:g.87981947_87981948del , CM000666.2:g.87981947_87981948del	GRCh38
NC_000004.11:g.88903099_88903100del , CM000666.1:g.88903099_88903100del	GRCh37
NC_000004.10:g.89122123_89122124del	NCBI36
NG_030362.1:g.11298_11299del

Transcript Alleles

HGVS	Amino-acid change
ENST00000508233.6:c.417+149_417+150del	ENSP00000422973.2:n.417+149_417+150del
ENST00000614857.5:c.540+149_540+150del	ENSP00000477824.2:n.540+149_540+150del
ENST00000681973.1:n.767+149_767+150del
ENST00000682026.1:n.493+149_493+150del
ENST00000682448.1:n.2026+149_2026+150del
ENST00000682554.1:n.1988+149_1988+150del
ENST00000682599.1:n.3028+149_3028+150del
ENST00000682627.1:n.460+149_460+150del
ENST00000682655.1:c.*110_*111del	ENSP00000508280.1:n.*110_*111del
ENST00000682865.1:n.824+149_824+150del
ENST00000683087.1:n.554+149_554+150del
ENST00000683168.1:n.1294+149_1294+150del
ENST00000683620.1:n.1722+149_1722+150del
ENST00000684106.1:n.2790+149_2790+150del
ENST00000684450.1:n.1599+149_1599+150del
ENST00000684710.1:n.1831+149_1831+150del
ENST00000395080.8:c.540+149_540+150del MANE Select	ENSP00000378517.3:n.540+149_540+150del
ENST00000237623.11:c.498+149_498+150del	ENSP00000237623.7:n.498+149_498+150del
ENST00000360804.4:c.459+149_459+150del	ENSP00000354042.4:n.459+149_459+150del
ENST00000395080.7:c.540+149_540+150del	ENSP00000378517.3:n.540+149_540+150del
ENST00000508233.5:c.417+149_417+150del	ENSP00000422973.1:n.417+149_417+150del
ENST00000509659.5:n.829+149_829+150del
ENST00000614857.4:c.474+149_474+150del	ENSP00000477824.1:n.474+149_474+150del
NM_000582.2:c.498+149_498+150del	NP_000573.1:n.498+149_498+150del
NM_001040058.1:c.540+149_540+150del	NP_001035147.1:n.540+149_540+150del
NM_001040060.1:c.459+149_459+150del	NP_001035149.1:n.459+149_459+150del
NM_001251829.1:c.417+149_417+150del	NP_001238758.1:n.417+149_417+150del
NM_001251830.1:c.579+149_579+150del	NP_001238759.1:n.579+149_579+150del
NM_001040058.2:c.540+149_540+150del MANE Select	NP_001035147.1:n.540+149_540+150del
NM_000582.3:c.498+149_498+150del	NP_000573.1:n.498+149_498+150del
NM_001040060.2:c.459+149_459+150del	NP_001035149.1:n.459+149_459+150del
NM_001251829.2:c.417+149_417+150del	NP_001238758.1:n.417+149_417+150del
NM_001251830.2:c.579+149_579+150del	NP_001238759.1:n.579+149_579+150del